REACTION OF ALPHA-BROMO KETONES WITH BIS(TRIETHYLSILYL)MERCURY AND BIS(TRIETHYLGERMYL)MERCURY

被引：1

作者：

GENDIN, DV

KRUGLAYA, OA

KALIKHMAN, ID

VYAZANKIN, NS

FURIN, GG

机构：

来源：

BULLETIN OF THE ACADEMY OF SCIENCES OF THE USSR DIVISION OF CHEMICAL SCIENCE | 1979年 / 28卷 / 10期

关键词：

D O I：

10.1007/BF00947581

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

1. The reaction of bis (triethylsilyl)mercury with α-bromoacetophenone, its halo-substituted derivatives, and 1-bromo-1-phenyl-2-propanone gave the corresponding triethylsilyl ethers of enols. In the case of bis(triethylgermyl)mercury, depending on the employed α-bromo ketone, either the enol ether or a mixture of the O- and C-germylation products is formed. © 1980 Plenum Publishing Corporation.

引用

页码：2192 / 2194

页数：3

共 6 条

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[2] ORGANOSILICON CHEMISTRY .3. REACTION OF BIS(TRIMETHYLSILYL)MERCURY WITH ARYL HALIDES [J].

FIELDS, R ;

HASZELDI.RN ;

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[3]

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[4] GERMANOTROPIC EQUILIBRIUM [J].

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[5]

RASMUSSEN JK, 1971, SYNTHESIS, P91

[6]

VYAZANKIN NS, 1964, DOKL AKAD NAUK SSSR+, V155, P830

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